Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:82033445-82033720 | Rare:108 | ||||
chr17:82089051-82089274 | Common:1; Rare:93; Clinvar:2; Clinvar (benign):2 | ||||
chr17:82092965-82093328 | Common:4; Rare:117; Clinvar:5; Clinvar (benign):4 | ||||
chr18:159462-159617 | Rare:32 | ||||
chr18:905730-905843 | Common:2; Rare:36 | ||||
chr18:906650-906806 | Common:1; Rare:30 | ||||
chr18:5237759-5238135 | Common:5; Rare:133 | ||||
chr18:39841376-39841755 | Common:3; Rare:73 | ||||
chr18:46028140-46028227 | Rare:25 | ||||
chr18:46759926-46760195 | Common:3; Rare:42 | ||||
chr18:55350707-55350905 | Common:1; Rare:45; Clinvar:1 | ||||
chr18:55419571-55419841 | Rare:40 | ||||
chr18:57352524-57352928 | Common:11; Rare:164 | ||||
chr18:57352955-57353013 | Rare:19 | ||||
chr18:57630168-57630297 | Common:3; Rare:35 |